510(k) K043527 ยท LRC Instrument, Ent Manual Surgical
RELIEVA SINUS BALLOON DILATION CATHETER
| Applicant | Exploramed Nc1, Inc., Mountain View CA, US |
| Decision | Substantially Equivalent, Apr 5, 2005 |
| Received | Dec 21, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K043527
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.